{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Fenton",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64931",
      "recalling_firm": "Progressive Medical Inc",
      "address_1": "997 Horan Dr",
      "address_2": "N/A",
      "postal_code": "63026-2401",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution including AR, AZ, CA, CO, FL, ID, IL, IN, KS, KY, LA, MA, MI, MN, MO, NE, OH, OK, OR, TN, TX, WA, and WI.",
      "recall_number": "Z-1351-2013",
      "product_description": "Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Coated Blade 2.50\" (6.40) Length, Product number P0012, Rx Only.  Sterilized by Radiation.  Manufactured for Progressive Medical, Inc., St. Louis, MO 63128.      Electrodes used in Electrosurgeries",
      "product_quantity": "150 boxes with 12 units each.",
      "reason_for_recall": "Product coatings require 510K approval.",
      "recall_initiation_date": "20130412",
      "center_classification_date": "20130522",
      "termination_date": "20140507",
      "report_date": "20130529",
      "code_info": "Lot numbers 071212-01,  082712-01 and 111212-04"
    }
  ]
}